Devoto Paola, Flore Giovanna, Longu Giorgio, Pira Luigi, Gessa Gian Luigi
B.B. Brodie Department of Neuroscience, University of Cagliari, Monserrato, Italy.
Synapse. 2003 Dec 1;50(3):200-5. doi: 10.1002/syn.10264.
Our recent studies suggest that extracellular dopamine (DA) in the cerebral cortex not only originates from dopaminergic terminals but is also coreleased with noradrenaline (NA) from noradrenergic terminals [Devoto et al. (2001) Mol Psychiatry 6:657-664]. To further clarify this issue, the concentrations of extracellular DA, its deaminated metabolite, 3,4-dihydroxyphenylacetic acid (DOPAC), and NA were compared by microdialysis in the medial prefrontal cortex (mPFC), an area densely innervated by NA and DA neurons, and in the occipital cortex (OCC), equally innervated by NA but receiving scarce DA projections. Moreover, the effect of the alpha(2)-adrenoceptor agonist clonidine locally perfused into the locus coeruleus (LC) on extracellular NA, DA, and DOPAC in the mPFC, OCC, and ventral striatum was investigated. Consistent with the homogeneous NA innervation, extracellular NA concentration was similar in both cortices, while extracellular DA in the OCC, in spite of the scarce DA afference in this area, was only 37% lower than in the mPFC; extracellular DOPAC in the OCC was 81% lower than in the mPFC. Consistent with its ability to inhibit NA neurons, clonidine (10 microM) reduced extracellular NA by about 65 and 80% in the OCC and the mPFC, respectively, but also reduced extracellular DA by 70 and 50% in the OCC and the mPFC, respectively. Clonidine reduced DOPAC in the OCC (by about 40%) but not in the mPFC. In the ventral striatum clonidine reduced NA (by 30%) but not DA and DOPAC. After inhibition of the DA and NA transporter, by perfusing 100 microM desmethyl-imipramine into the mPFC, clonidine perfusion into the LC reduced extracellular NA and DA in the mPFC by about 50%. The results indicate that most of extracellular DA in the OCC and a significant portion in the mPFC reflect the activity of NA neurons and support the hypothesis that extracellular DA in the cerebral cortex may originate not only from DA but also from NA neurons.
我们最近的研究表明,大脑皮质中的细胞外多巴胺(DA)不仅来源于多巴胺能终末,还与去甲肾上腺素(NA)从去甲肾上腺素能终末共同释放[德沃托等人(2001年)《分子精神病学》6:657 - 664]。为了进一步阐明这个问题,通过微透析比较了内侧前额叶皮质(mPFC)和枕叶皮质(OCC)中细胞外DA、其脱氨基代谢产物3,4 - 二羟基苯乙酸(DOPAC)和NA的浓度。mPFC是一个由NA和DA神经元密集支配的区域,而OCC同样由NA支配,但接受的DA投射很少。此外,还研究了局部灌注到蓝斑(LC)的α₂ - 肾上腺素能受体激动剂可乐定对mPFC、OCC和腹侧纹状体中细胞外NA、DA和DOPAC的影响。与均匀的NA支配一致,两个皮质中的细胞外NA浓度相似,而OCC中的细胞外DA,尽管该区域的DA传入很少,但仅比mPFC低37%;OCC中的细胞外DOPAC比mPFC低81%。与它抑制NA神经元的能力一致,可乐定(10微摩尔)使OCC和mPFC中的细胞外NA分别降低了约65%和80%,但也使OCC和mPFC中的细胞外DA分别降低了70%和50%。可乐定使OCC中的DOPAC降低(约40%),但未使mPFC中的DOPAC降低。在腹侧纹状体中,可乐定使NA降低(30%),但未使DA和DOPAC降低。在向mPFC灌注100微摩尔去甲丙咪嗪抑制DA和NA转运体后,向LC灌注可乐定使mPFC中的细胞外NA和DA降低了约50%。结果表明,OCC中大部分细胞外DA以及mPFC中相当一部分细胞外DA反映了NA神经元的活动,并支持大脑皮质中细胞外DA可能不仅来源于DA神经元,还来源于NA神经元的假说。